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Active, not recruiting Phase 3 Interventional

Assessing Durvalumab and FLOT Chemotherapy in Resectable Gastric and Gastroesophageal Junction Cancer

ClinicalTrials.gov ID: NCT04592913

Public ClinicalTrials.gov record NCT04592913. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 11:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled, Phase III Study of Neoadjuvant-Adjuvant Durvalumab and FLOT Chemotherapy Followed by Adjuvant Durvalumab in Patients With Resectable Gastric and Gastroesophageal Junction Cancer (GC/GEJC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Global Study of Neoadjuvant-Adjuvant Durvalumab or Placebo and FLOT Chemotherapy Followed by Adjuvant Durvalumab or Placebo in Patients with Resectable Gastric and Gastroesophageal Cancer (GC/GEJC) (MATTERHORN).

Study identification

NCT ID
NCT04592913
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
957 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 200 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 17, 2020 (Actual)
Primary completion
Dec 20, 2024 (Actual)
Completion
Sep 27, 2027 (Estimated)
Last update posted
Dec 24, 2025

2020 – 2027

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Research Site Duarte California 91010 —
Research Site Los Angeles California 90027 —
Research Site Los Angeles California 90095 —
Research Site Sylmar California 91342 —
Research Site St. Petersburg Florida 33705 —
Research Site Tallahassee Florida 32308 —
Research Site West Palm Beach Florida 33401 —
Research Site Fort Wayne Indiana 46804 —
Research Site Louisville Kentucky 40217 —
Research Site Boston Massachusetts 02215 —
Research Site New York New York 10065 —
Research Site Rochester New York 14642 —
Research Site Nashville Tennessee 37203 —
Research Site Dallas Texas 75390 —
Research Site Lancaster Texas 75216 —
Research Site Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 140 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04592913, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 24, 2025 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04592913 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →